{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Salvany S"],"funding":["Ministerio de Ciencia e Innovación","Ministerio de Educación, Cultura y Deporte"],"pagination":["e13078"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9616096"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["32(6)"],"pubmed_abstract":["Early misfolded superoxide dismutase 1 (mfSOD1) accumulation, motor neuron (MN) degeneration, and microgliosis are hallmark pathological features in SOD1<sup>G93A</sup> amyotrophic lateral sclerosis (ALS) mice. Because of the different vulnerabilities of distinct MN subtypes, degenerating and surviving MNs coexist in different proportions during disease progression. By examining the expression of misfolded conformers of SOD1 using specific antibodies, we defined distinct MN phenotypes that were evaluated during disease progression and the local neuroinflammatory reaction. The most severe phenotype corresponded to somata of fast-twitch subtype MNs, which exhibited highly positive mfSOD1 immunostaining and an extreme degree of vacuolar degeneration. Vacuoles, which are of mitochondrial origi"],"journal":["Brain pathology (Zurich, Switzerland)"],"pubmed_title":["Accumulation of misfolded SOD1 outlines distinct patterns of motor neuron pathology and death during disease progression in a SOD1<sup>G93A</sup> mouse model of amyotrophic lateral sclerosis."],"pmcid":["PMC9616096"],"funding_grant_id":["RTI2018-099278-B-I00","RTI2018‐099278‐B‐I00"],"pubmed_authors":["Caldero J","Esquerda JE","Piedrafita L","Gras S","Salvany S","Casanovas A"],"additional_accession":[]},"is_claimable":false,"name":"Accumulation of misfolded SOD1 outlines distinct patterns of motor neuron pathology and death during disease progression in a SOD1<sup>G93A</sup> mouse model of amyotrophic lateral sclerosis.","description":"Early misfolded superoxide dismutase 1 (mfSOD1) accumulation, motor neuron (MN) degeneration, and microgliosis are hallmark pathological features in SOD1<sup>G93A</sup> amyotrophic lateral sclerosis (ALS) mice. Because of the different vulnerabilities of distinct MN subtypes, degenerating and surviving MNs coexist in different proportions during disease progression. By examining the expression of misfolded conformers of SOD1 using specific antibodies, we defined distinct MN phenotypes that were evaluated during disease progression and the local neuroinflammatory reaction. The most severe phenotype corresponded to somata of fast-twitch subtype MNs, which exhibited highly positive mfSOD1 immunostaining and an extreme degree of vacuolar degeneration. Vacuoles, which are of mitochondrial origi","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Nov","modification":"2025-04-19T04:20:26.099Z","creation":"2025-04-19T04:20:26.099Z"},"accession":"S-EPMC9616096","cross_references":{"pubmed":["35584812"],"doi":["10.1111/bpa.13078"]}}